It is phenotype.
The genotype AA represents a homozygous dominant genotype. The capital letter "A" represents the dominant allele, while the lowercase letter "a" would represent the recessive allele. If both dominant alleles are present in a genotype (homozygous dominant) then the phenotype is "A" phenotype. If one dominant allele and one recessive allele are present (heterozygous dominant) then the phenotype is "A". Finally, if both recessive alleles "a" are present (homozygous recessive) then the phenotype is "a". Therefore, the answer to your question is the genotype AA would result in an "A" phenotype because the genotype is homozygous dominant.
An organism's genotype is its genetic identity. The genotype is comprised of all the genetic material inherited from both parents. The genotype is what "tells" each individual cell how to function. The phenotype is the physical expression of an organism's genotype. For example, if a person's genotype for eye color is one dominant allele for brown and one recessive for blue, then the individual's phenotype would be their actual eye color which in this case would be brown.
You just know
Nope! TT is the dominant phenotype (what ever it may be) and tt is the recessive phenotype (what ever that may be).So say T is the allele for Tall plants, t is the allele for short plants. TT would be show the tall phenotype while tt would show the short phenotype. If the genotype was Tt, the phenotype would be tall as well because the T is dominant and masks the phenotype of t (short plants).
The term that describes inherited traits that are visible would be the organisms phenotype. The genotype would be the genes that make the traits.
If A represents a dominant allele, then the AA genotype would produce the dominant phenotype.
The genotype AA represents a homozygous dominant genotype. The capital letter "A" represents the dominant allele, while the lowercase letter "a" would represent the recessive allele. If both dominant alleles are present in a genotype (homozygous dominant) then the phenotype is "A" phenotype. If one dominant allele and one recessive allele are present (heterozygous dominant) then the phenotype is "A". Finally, if both recessive alleles "a" are present (homozygous recessive) then the phenotype is "a". Therefore, the answer to your question is the genotype AA would result in an "A" phenotype because the genotype is homozygous dominant.
An organism's genotype is its genetic identity. The genotype is comprised of all the genetic material inherited from both parents. The genotype is what "tells" each individual cell how to function. The phenotype is the physical expression of an organism's genotype. For example, if a person's genotype for eye color is one dominant allele for brown and one recessive for blue, then the individual's phenotype would be their actual eye color which in this case would be brown.
If both parents have the same phenotype, but the offspring did not share that phenotype, then it is likely that the parents have a dominant phenotype, but the offspring has a recessive phenotype, which means that the offpring's genotype would be homozygous recessive, and it's parents' genotypes would be heterozygous. For example, the parents may both have the genotype Bb, which gives them black fur. Approximately 25% of their offspring should have the genotype bb, which gives them the phenotype of white fur.
Genotype codes for phenotype. Phenotype is the expressed trait, for example, black fur. The genome that codes for black fur would be BB for example
It's a genotype. The phenotype is a physical manifestation of the genotype, which means that it's what happens on the outside because an organism has the gene. An example of a phenotype would be if someone had blue eyes or something. The genotype is the two-letter abbreviation thingy.
You just know
GG would be a dominant phenotype
If both parents have the same phenotype, but the offspring did not share that phenotype, then it is likely that the parents have a dominant phenotype, but the offspring has a recessive phenotype, which means that the offpring's genotype would be homozygous recessive, and it's parents' genotypes would be heterozygous. For example, the parents may both have the genotype Bb, which gives them black fur. Approximately 25% of their offspring should have the genotype bb, which gives them the phenotype of white fur.
For monohybrid cross the genotype ratio in f2 generation would be 1:2:1 and phenotype ratio would be 3: 1
Are you talking about phenotype or genotype? Phenotype is the expression of the genotype. Genotype is what you inherited. Phenotype is what you see. Homozygous is the same. Heterozygous is different. If you inherit one allele for blue eyes and one allele for brown eyes, your phenotype should be brown eyes. Your genotype would be brown eyes, blue eyes. You would have a heterozygous genotype.
homozygous dominant is the genotype. hypothetically, if the gene was for the color purple in a flower, the phenotype would be purple, while the genotype would be homozygous dominant AKA Pp.